Fast saccharide mapping method for quality consistency evaluation of commercial xylooligosaccharides collected in China

Due to the extensive use of xylooligosaccharides (XOS) as functional food ingredients, many inferior goods and even adulterants are generally found in the market, which may pose a health hazard to certain populations. Chromatography method such as high-performance liquid chromatography (HPLC) and hi...

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Bibliographic Details
Main Authors: Chen, C. (Author), Chen, L. (Author), Deng, Y. (Author), Han, B. (Author), Li, S. (Author), Zhao, J. (Author)
Format: Article
Language:English
Published: Xi'an Jiaotong University 2021
Subjects:
Online Access:View Fulltext in Publisher
LEADER 02773nam a2200409Ia 4500
001 10.1016-j.jpha.2020.08.013
008 220427s2021 CNT 000 0 und d
020 |a 20951779 (ISSN) 
245 1 0 |a Fast saccharide mapping method for quality consistency evaluation of commercial xylooligosaccharides collected in China 
260 0 |b Xi'an Jiaotong University  |c 2021 
856 |z View Fulltext in Publisher  |u https://doi.org/10.1016/j.jpha.2020.08.013 
520 3 |a Due to the extensive use of xylooligosaccharides (XOS) as functional food ingredients, many inferior goods and even adulterants are generally found in the market, which may pose a health hazard to certain populations. Chromatography method such as high-performance liquid chromatography (HPLC) and high-performance thin-layer chromatography (HPTLC) is traditionally applied for the quality analysis of XOS. However, it is time consuming due to the prolonged separation and pre- or post- derivatization procedure. In this study, a fast saccharide mapping method based on matrix-assisted laser desorption/time-of-flight mass spectrometry (MALDI-TOF-MS) was developed for the quality consistency analysis of 22 batches of XOS collected from different manufacturers in China. The time needed for saccharides analysis using MALDI-MS was less than 30 min for one plate, at least 6 times faster than that by the traditional HPTLC chromatography method. In addition, MALDI-MS possessed higher resolution for XOS with DP4-DP7 based on the difference of m/z, which is hardly separated using HPTLC. The results showed that XOS were present only in samples XY01-XY11, samples XY12-XY14 only consisted of hex oligosaccharides, and samples XY15-XY22 were free of oligosaccharides. These indicate that the quality consistency of XOS products in the China market was poor, which should be carefully investigated. © 2020 Xi'an Jiaotong University 
650 0 4 |a Article 
650 0 4 |a China 
650 0 4 |a data analysis software 
650 0 4 |a food ingredient 
650 0 4 |a functional food 
650 0 4 |a high performance thin layer chromatography 
650 0 4 |a MALDI-MS 
650 0 4 |a mass fragmentography 
650 0 4 |a matrix assisted laser desorption ionization time of flight mass spectrometry 
650 0 4 |a oligosaccharide 
650 0 4 |a quality control 
650 0 4 |a Quality control 
650 0 4 |a Saccharide mapping 
650 0 4 |a separation technique 
650 0 4 |a time 
650 0 4 |a unclassified drug 
650 0 4 |a xylooligosaccharide 
650 0 4 |a Xylooligosaccharides 
700 1 |a Chen, C.  |e author 
700 1 |a Chen, L.  |e author 
700 1 |a Deng, Y.  |e author 
700 1 |a Han, B.  |e author 
700 1 |a Li, S.  |e author 
700 1 |a Zhao, J.  |e author 
773 |t Journal of Pharmaceutical Analysis